Chen YJ - Search Results

1

Identification and characterization of three inherited genomic copy number variations associated with familial schizophrenia.

Liao HM, Chao YL, Huang AL, Cheng MC, Chen YJ, Lee KF, Fang JS, Hsu CH, Chen CH. Liao HM, et al. Among authors: chen yj, chen ch. Schizophr Res. 2012 Aug;139(1-3):229-36. doi: 10.1016/j.schres.2012.05.015. Epub 2012 Jun 7. Schizophr Res. 2012. PMID: 22682706

2

Clinical and molecular characterization of three genomic rearrangements at chromosome 22q13.3 associated with autism spectrum disorder.

Chen CH, Chen HI, Liao HM, Chen YJ, Fang JS, Lee KF, Gau SS. Chen CH, et al. Among authors: chen hi, chen yj. Psychiatr Genet. 2017 Feb;27(1):23-33. doi: 10.1097/YPG.0000000000000151. Psychiatr Genet. 2017. PMID: 27846046

3

Clinical and molecular characterization of a transmitted reciprocal translocation t(1;12)(p32.1;q21.3) in a family co-segregating with mental retardation, language delay, and microcephaly.

Liao HM, Fang JS, Chen YJ, Wu KL, Lee KF, Chen CH. Liao HM, et al. Among authors: chen yj, chen ch. BMC Med Genet. 2011 May 20;12:70. doi: 10.1186/1471-2350-12-70. BMC Med Genet. 2011. PMID: 21595979 Free PMC article.

4

The database of chromosome imbalance regions and genes resided in lung cancer from Asian and Caucasian identified by array-comparative genomic hybridization.

Lo FY, Chang JW, Chang IS, Chen YJ, Hsu HS, Huang SF, Tsai FY, Jiang SS, Kanteti R, Nandi S, Salgia R, Wang YC. Lo FY, et al. Among authors: chen yj. BMC Cancer. 2012 Jun 12;12:235. doi: 10.1186/1471-2407-12-235. BMC Cancer. 2012. PMID: 22691236 Free PMC article.

5

Attitudes toward Pursuing Genetic Testing among Parents of Children with Autism Spectrum Disorder in Taiwan: A Qualitative Investigation.

Zhang Z, Kramer J, Wang H, Chen WJ, Huang TY, Chen YJ, Tseng TS, Chen LS. Zhang Z, et al. Among authors: chen yj, chen wj, chen ls. Int J Environ Res Public Health. 2021 Dec 23;19(1):118. doi: 10.3390/ijerph19010118. Int J Environ Res Public Health. 2021. PMID: 35010379 Free PMC article.

6

Mosaic ring chromosome 18, ring chromosome 18 duplication/deletion and disomy 18: perinatal findings and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization.

Chen CP, Kuo YT, Lin SP, Su YN, Chen YJ, Hsueh RY, Lin YH, Wu PC, Lee CC, Chen YT, Wang W. Chen CP, et al. Among authors: chen yj, chen yt. Taiwan J Obstet Gynecol. 2010 Sep;49(3):327-32. doi: 10.1016/S1028-4559(10)60069-1. Taiwan J Obstet Gynecol. 2010. PMID: 21056319 Free article.

7

Analysis of genetic aberrations in uterine adenomyosis using comparative genomic hybridization.

Wang PH, Shyong WY, Lin CH, Chen YJ, Li YF, Chao HT, Yuan CC. Wang PH, et al. Among authors: chen yj. Anal Quant Cytol Histol. 2002 Feb;24(1):1-6. Anal Quant Cytol Histol. 2002. PMID: 11865944

8

Comparative genomic hybridization-assisted prenatal diagnosis of a de novo inverted duplication of chromosome 10q. A case report.

Chen CK, Chang SD, Chen YJ, Hsueh DW, Soong YK. Chen CK, et al. Among authors: chen yj. J Reprod Med. 2003 May;48(5):391-4. J Reprod Med. 2003. PMID: 12815917

9

Copy number changes of target genes in chromosome 3q25.3-qter of esophageal squamous cell carcinoma: TP63 is amplified in early carcinogenesis but down-regulated as disease progressed.

Yen CC, Chen YJ, Pan CC, Lu KH, Chen PC, Hsia JY, Chen JT, Wu YC, Hsu WH, Wang LS, Huang MH, Huang BS, Hu CP, Chen PM, Lin CH. Yen CC, et al. Among authors: chen yj, chen pc, chen pm, chen jt. World J Gastroenterol. 2005 Mar 7;11(9):1267-72. doi: 10.3748/wjg.v11.i9.1267. World J Gastroenterol. 2005. PMID: 15761962 Free PMC article.

10

High mitochondrial DNA copy number and bioenergetic function are associated with tumor invasion of esophageal squamous cell carcinoma cell lines.

Lin CS, Lee HT, Lee SY, Shen YA, Wang LS, Chen YJ, Wei YH. Lin CS, et al. Among authors: chen yj. Int J Mol Sci. 2012;13(9):11228-11246. doi: 10.3390/ijms130911228. Epub 2012 Sep 10. Int J Mol Sci. 2012. PMID: 23109849 Free PMC article.

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